Infliximab for steroid-refractory acute GVHD: A case series

被引:67
作者
Jacobsohn, DA
Hallick, J
Anders, V
McMillan, S
Morris, L
Vogelsang, GB
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Pediat, Chicago, IL 60611 USA
[2] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[3] Blood & Marrow Transplant Grp Georgia, Atlanta, GA USA
关键词
graft-versus-host disease; TNF-alpha; infliximab;
D O I
10.1002/ajh.10392
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acute and chronic graft-versus-host disease (GVHD) remain major barriers to successful hematopoietic stem cell transplantation (SCT). TNF-alpha has been implicated in the pathogenesis of GVHD and TNF-alpha blockade has been explored for treatment of GVHD. The development of a chimeric mouse/human monoclonal antibody (infliximab) which binds to cells producing TNF-alpha, allowing for not only the neutralization of TNF-alpha but also lysis of the cells producing the TNF-alpha, makes this an attractive drug to explore in GVHD. We report on 11 patients with acute GVHD who were treated with infliximab after failing other therapies. The survival was very poor, in keeping with previously published reports of steroid-refractory acute GVHD. Two patients with severe diarrhea from acute GI GVHD resolved their symptoms after treatment with infliximab. Only these two patients survived. It appears that of all acute GVHD manifestations, gastrointestinal GVHD may be more responsive to treatment with infliximab than others. Caution is recommended when using this agent since it may exacerbate active infections, particularly aspergillosis. Furthermore, we do not know the correct dose or schedule to use with this drug. Given these data, controlled studies assessing dose and timing of administration may be warranted to study infliximab in acute GVHD. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:119 / 124
页数:6
相关论文
共 24 条
[1]   Poor outcome in steroid-refractory graft-versus-host disease with antithymocyte globulin treatment [J].
Arai, S ;
Margolis, J ;
Zaburak, M ;
Anders, V ;
Vogelsang, GB .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2002, 8 (03) :155-160
[2]  
CAVENDER DE, 1986, J IMMUNOL, V136, P203
[3]  
CHANG RJ, 1986, J IMMUNOL, V137, P2853
[4]   Tumor necrosis factor-α production to lipopolysaccharide stimulation by donor cells predicts the severity of experimental acute graft-versus-host disease [J].
Cooke, KR ;
Hill, GR ;
Crawford, JM ;
Bungard, D ;
Brinson, YS ;
Delmonte, J ;
Ferrara, JLM .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (10) :1882-1891
[5]   Role of tumor necrosis factor-alpha inhibition with inflixiMAB in cancer therapy and hematopoietic stem cell transplantation [J].
Couriel, DR ;
Hicks, K ;
Giralt, S ;
Champlin, RE .
CURRENT OPINION IN ONCOLOGY, 2000, 12 (06) :582-587
[6]  
DEEG HJ, 1990, BONE MARROW TRANSPL, V6, P1
[7]  
DICKINSON AM, 1991, BONE MARROW TRANSPL, V7, P209
[8]  
Ferrara J L, 1999, Biol Blood Marrow Transplant, V5, P347, DOI 10.1016/S1083-8791(99)70011-X
[9]   Differential effects of anti-Fas ligand and anti-tumor necrosis factor α antibodies on acute graft-versus-host disease pathologies [J].
Hattori, K ;
Hirano, T ;
Miyajima, H ;
Yamakawa, N ;
Tateno, M ;
Oshimi, K ;
Kayagaki, N ;
Yagita, H ;
Okumura, K .
BLOOD, 1998, 91 (11) :4051-4055
[10]   The primacy of the gastrointestinal tract as a target organ of acute graft-versus-host disease: rationale for the use of cytokine shields in allogeneic bone marrow transplantation [J].
Hill, GR ;
Ferrara, JLM .
BLOOD, 2000, 95 (09) :2754-2759